Variant report

Variant	esv1834762
Chromosome Location	chr12:40496733-40499934
allele	n/a
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

TF binding
region (count:378)
CpG islands
(count:245)
Chromatin interactive
region (count:4)
LncRNA
region (count:0)
Mature miRNA
region (count: 0)
miRNA target
sites (count:0)

(count:378 , 50 per page) page: 1 2 3 4 5 6 7 8

No.	Transcrition factor	Chromosome Location	Cell Line	Cell type	Cell Stage	Matched TF binding sites
1	ARID3A	chr12:40498779-40498912	K562	blood:	n/a	n/a
2	ARID3A	chr12:40498119-40498288	K562	blood:	n/a	n/a
3	ATF3	chr12:40499744-40499987	K562	blood:	n/a	chr12:40499976-40499985
4	BACH1	chr12:40499710-40499852	H1-hESC	embryonic stem cell:	n/a	n/a
5	BACH1	chr12:40498670-40498870	K562	blood:	n/a	n/a
6	BACH1	chr12:40498672-40498821	H1-hESC	embryonic stem cell:	n/a	n/a
7	BHLHE40	chr12:40499733-40500047	A549	lung:	n/a	chr12:40499900-40499909
8	BHLHE40	chr12:40498581-40500322	K562	blood:	n/a	chr12:40499900-40499909
9	BHLHE40	chr12:40499729-40500060	HepG2	liver:	n/a	chr12:40499900-40499909
10	BHLHE40	chr12:40499148-40500152	GM12878	blood:	n/a	chr12:40499900-40499909
11	BHLHE40	chr12:40498650-40500176	HepG2	liver:	n/a	chr12:40499900-40499909
12	CBX3	chr12:40498540-40498991	K562	blood:	n/a	n/a
13	CCNT2	chr12:40498953-40500070	K562	blood:	n/a	n/a
14	CEBPB	chr12:40499734-40500440	Hela-S3	cervix:	n/a	n/a
15	CEBPD	chr12:40499709-40499945	HepG2	liver:	n/a	n/a
16	CHD1	chr12:40499504-40499654	H1-hESC	embryonic stem cell:	n/a	n/a
17	CHD1	chr12:40499382-40499523	GM12878	blood:	n/a	n/a
18	CHD2	chr12:40499108-40499848	K562	blood:	n/a	n/a
19	CHD2	chr12:40498606-40499137	GM12878	blood:	n/a	chr12:40498850-40498860
20	CHD2	chr12:40498701-40500266	Hela-S3	cervix:	n/a	chr12:40498850-40498860 chr12:40499881-40499891 chr12:40499847-40499857
21	CHD2	chr12:40499445-40499943	GM12878	blood:	n/a	chr12:40499881-40499891 chr12:40499847-40499857
22	CHD2	chr12:40498723-40498889	K562	blood:	n/a	chr12:40498850-40498860
23	CHD2	chr12:40499657-40499819	HepG2	liver:	n/a	n/a
24	CREB1	chr12:40499618-40500115	A549	lung:	n/a	n/a
25	CREB1	chr12:40499005-40500250	HepG2	liver:	n/a	n/a
26	CREB1	chr12:40499023-40499614	A549	lung:	n/a	n/a
27	CTCF	chr12:40499340-40499490	AG04449	skin:	n/a	n/a
28	CTCF	chr12:40499340-40499490	SK-N-SH_RA	brain:	n/a	n/a
29	CTCF	chr12:40499740-40499890	GM12872	blood:	n/a	n/a
30	CTCF	chr12:40499200-40499350	AG09319	gingival:	n/a	n/a
31	CTCF	chr12:40499176-40499179	MCF-7	breast:	n/a	n/a
32	CTCF	chr12:40499560-40499710	HUVEC	blood vessel:	n/a	n/a
33	CTCF	chr12:40499229-40499247	MCF-7	breast:	n/a	n/a
34	CTCF	chr12:40499360-40499510	Hela-S3	cervix:	n/a	n/a
35	CTCF	chr12:40499761-40499948	K562	blood:	n/a	n/a
36	CTCF	chr12:40499380-40499530	GM12865	blood:	n/a	n/a
37	CTCF	chr12:40499300-40499450	GM12871	blood:	n/a	n/a
38	CTCF	chr12:40499040-40499190	SAEC	small airway:	n/a	n/a
39	CTCF	chr12:40499560-40499710	AG04450	lung:	n/a	n/a
40	CTCF	chr12:40499680-40499830	GM12869	blood:	n/a	n/a
41	CTCF	chr12:40499740-40499890	SK-N-SH_RA	brain:	n/a	n/a
42	CTCF	chr12:40499480-40499630	GM12867	blood:	n/a	n/a
43	CTCF	chr12:40499380-40499530	GM12871	blood:	n/a	n/a
44	CTCF	chr12:40499289-40499303	GM19239	blood:	n/a	n/a
45	CTCF	chr12:40499830-40500038	GM12878	blood:	n/a	n/a
46	CTCF	chr12:40499120-40499270	HCFaa	heart:	n/a	n/a
47	CTCF	chr12:40499779-40499961	Spleen_OC	spleen:	n/a	n/a
48	CTCF	chr12:40499380-40499530	HCPEpiC	choroid plexus:	n/a	n/a
49	CTCF	chr12:40499180-40499313	MCF-7	breast:	n/a	n/a
50	CTCF	chr12:40499561-40499599	Spleen_OC	spleen:	n/a	n/a

(count:245 , 50 per page) page: 1 2 3 4 5

No.	Chromosome Location	Cell Line	Cell type	Cell Stage
1	chr12:40499262-40499312	HCF	heart:	n/a
2	chr12:40499262-40499312	HCF	heart:	n/a
3	chr12:40499262-40499312	PANC-1	pancreas:	n/a
4	chr12:40499262-40499312	RPTEC	kidney:	n/a
5	chr12:40499811-40499861	MCF10A-Er-Src	breast:	n/a
6	chr12:40499262-40499312	NB4	blood:	n/a
7	chr12:40497575-40497625	HRE	kidney:	n/a
8	chr12:40499262-40499312	NT2-D1	testis:	n/a
9	chr12:40499262-40499312	HepG2	liver:	n/a
10	chr12:40497575-40497625	A549	lung:	n/a
11	chr12:40497575-40497625	K562	blood:	n/a
12	chr12:40499811-40499861	Hela-S3	cervix:	n/a
13	chr12:40499811-40499861	NH-A	brain:	n/a
14	chr12:40499623-40499673	GM19239	blood:	n/a
15	chr12:40499811-40499861	AG10803	skin:	n/a
16	chr12:40497575-40497625	MCF10A-Er-Src	breast:	n/a
17	chr12:40497575-40497625	HRPEpiC	eye:	n/a
18	chr12:40497575-40497625	MCF-7	breast:	n/a
19	chr12:40499262-40499312	HUVEC	blood vessel:	n/a
20	chr12:40499623-40499673	Hepatocyte	liver:	n/a
21	chr12:40497575-40497625	HPAEpiC	pulmonary alveolar:	n/a
22	chr12:40499262-40499312	Hela-S3	cervix:	n/a
23	chr12:40497575-40497625	PANC-1	pancreas:	n/a
24	chr12:40499262-40499312	HMEC	breast:	n/a
25	chr12:40497575-40497625	GM12891	blood:	n/a
26	chr12:40497575-40497625	Hela-S3	cervix:	n/a
27	chr12:40499262-40499312	AG04450	lung:	fetal
28	chr12:40497575-40497625	AG09309	skin:	n/a
29	chr12:40497575-40497625	SK-N-SH	brain:	n/a
30	chr12:40497575-40497625	HEEpiC	esophagus:	n/a
31	chr12:40497575-40497625	GM19239	blood:	n/a
32	chr12:40499262-40499312	IMR90	lung:	fetal
33	chr12:40499811-40499861	BE2_C	brain:	n/a
34	chr12:40499262-40499312	Hepatocyte	liver:	n/a
35	chr12:40497575-40497625	BE2_C	brain:	n/a
36	chr12:40499623-40499673	CMK	blood:	n/a
37	chr12:40499623-40499673	HRPEpiC	eye:	n/a
38	chr12:40499623-40499673	HepG2	liver:	n/a
39	chr12:40499262-40499312	AG09309	skin:	n/a
40	chr12:40499623-40499673	HPAEpiC	pulmonary alveolar:	n/a
41	chr12:40497575-40497625	HAEpiC	amniotic membrane:	n/a
42	chr12:40497575-40497625	Hepatocyte	liver:	n/a
43	chr12:40499811-40499861	HEK293	kidney:	embryo
44	chr12:40499623-40499673	AoSMC	blood vessel:	n/a
45	chr12:40499623-40499673	AG04450	lung:	fetal
46	chr12:40499811-40499861	HMEC	breast:	n/a
47	chr12:40499262-40499312	GM06990	blood:	n/a
48	chr12:40499811-40499861	U87	brain:	n/a
49	chr12:40499262-40499312	SK-N-MC	brain:	n/a
50	chr12:40499623-40499673	GM12892	blood:	n/a

(count:4 , 50 per page) page: 1

No.	Distal block	Cell Line	Cell type
1	chr12:40495644..40497821-chr12:40498343..40500336,2	MCF-7	breast:
2	chr12:40494859..40496427-chr12:40496570..40499467,2	MCF-7	breast:
3	chr11:62607295..62609623-chr12:40497021..40499693,2	MCF-7	breast:
4	chr12:39835235..39837376-chr12:40497652..40499874,2	K562	blood:

No data

Variant related genes	Relation type
SLC2A13	TF binding region
SLC2A13	CpG island
ENSG00000139116	chromatin interactions
ENSG00000133316	chromatin interactions
ENSG00000252974	chromatin interactions
ENSG00000151229	chromatin interactions

Extended variants
information (count: 134 )
Associated
traits (count: 56 )

Variant overlapped rSNPs/rCNVs (count:134 , 50 per page) page: 1 2 3

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	rs17489631	chr12:40496733-40496734	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
2	rs149391266	chr12:40496734-40496735	Weak transcription Enhancers Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
3	rs543207862	chr12:40496817-40496818	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
4	rs561584950	chr12:40496833-40496834	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
5	rs17489638	chr12:40496850-40496851	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
6	rs554059229	chr12:40496859-40496860	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
7	rs184630726	chr12:40496860-40496861	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
8	rs559459969	chr12:40496912-40496913	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
9	rs564141093	chr12:40496924-40496925	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
10	rs138504155	chr12:40496925-40496926	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
11	rs552062154	chr12:40496929-40496930	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
12	rs570362279	chr12:40496931-40496932	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
13	rs528168811	chr12:40496949-40496950	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
14	rs537782901	chr12:40496996-40496997	Weak transcription Enhancers Flanking Active TSS Active TSS	Chromatin interactive region	1 gene(s)	Overlapped CNVs	n/a
15	rs549582727	chr12:40497042-40497043	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
16	rs567879413	chr12:40497061-40497062	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
17	rs546752284	chr12:40497091-40497092	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
18	rs10784370	chr12:40497095-40497096	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	mRNA abundance
19	rs535491295	chr12:40497122-40497123	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
20	rs189417620	chr12:40497131-40497132	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
21	rs550600795	chr12:40497176-40497177	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
22	rs565501024	chr12:40497179-40497180	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
23	rs539420197	chr12:40497181-40497182	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
24	rs114611401	chr12:40497209-40497210	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
25	rs575919050	chr12:40497265-40497266	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
26	rs543344122	chr12:40497287-40497288	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
27	rs193047568	chr12:40497368-40497369	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
28	rs573800913	chr12:40497376-40497377	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
29	rs55689602	chr12:40497415-40497416	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
30	rs115355693	chr12:40497469-40497470	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
31	rs28365178	chr12:40497497-40497498	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a
32	rs76157149	chr12:40497508-40497509	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
33	rs79605372	chr12:40497510-40497511	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
34	rs545412582	chr12:40497513-40497514	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
35	rs563708869	chr12:40497535-40497536	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
36	rs185219609	chr12:40497536-40497537	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
37	rs531209804	chr12:40497576-40497577	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
38	rs144076260	chr12:40497603-40497604	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
39	rs374646975	chr12:40497615-40497616	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
40	rs189669457	chr12:40497643-40497644	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	2 gene(s)	Overlapped CNVs	n/a
41	rs12371122	chr12:40497719-40497720	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
42	rs17489652	chr12:40497731-40497732	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
43	rs539762656	chr12:40497732-40497733	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
44	rs547133070	chr12:40497756-40497757	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
45	rs201151994	chr12:40497781-40497782	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
46	rs139423348	chr12:40497782-40497783	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
47	rs181268610	chr12:40497788-40497789	Enhancers Weak transcription Flanking Active TSS Active TSS	Chromatin interactive region	4 gene(s)	Overlapped CNVs	n/a
48	rs557312001	chr12:40497833-40497834	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
49	rs186731710	chr12:40497842-40497843	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	Overlapped CNVs	n/a
50	rs931207	chr12:40497883-40497884	Active TSS Enhancers Weak transcription Flanking Active TSS Bivalent/Poised TSS	Chromatin interactive region	3 gene(s)	LD-proxies of rSNP Overlapped rCNV	n/a

Variant related diseases (count:56)

Disease	PMID	Source
Chronic lymphocytic leukemia	21546498	CNVD
Seminomas	18059402	CNVD
Wilms tumour	21544195	CNVD
Esophageal cancer	21851588	CNVD
Lung cancer	20668451	CNVD
Breast cancer	20668451	CNVD
Cancer	20668451	CNVD
Ovarian cancer	20668451	CNVD
Pancreas cancer	20668451	CNVD
Prostate cancer	20668451	CNVD
Ewing''s sarcoma	21437220	CNVD
Testicular germ cell tumor	18059402	CNVD
Medulloblastoma	21979893	CNVD
Malaria	21533027	CNVD
Chronic lymphocytic leukemia	22228453	CNVD
Basal cell lymphoma	17053054	CNVD
Chronic lymphocytic leukemia	21670202	CNVD
Ewing''s sarcoma	17952124	CNVD
Acute lymphoblastic leukemia	20435627	CNVD
Hodgkin''s lymphoma	17606441	CNVD
Thoracic aortic aneurysm	21092924	CNVD
Autism	22495311	CNVD
Cancer	20164919	CNVD
Neurodevelopmental disorder	22521361	CNVD
Acute lymphoblastic leukemia	21390130	CNVD
T-cell prolymphocytic leukemia	19278963	CNVD
T-cell prolymphocytic leukemia	17713554	CNVD
Renal cell carcinoma	18194544	CNVD
Breast cancer	21949216	CNVD
Carcinoma ex pleomorphic adenoma	18828159	CNVD
Acute myeloid leukemia	16864856	CNVD
Cancer	21637783	CNVD
Glioblastoma multiforme	21080181	CNVD
Renal cell carcinoma	19461508	CNVD
Burkitt''s lymphoma	18698080	CNVD
Astrocytoma	17387387	CNVD
Breast cancer	21264507	CNVD
Glioblastoma multiforme	19960244	CNVD
Gastrointestinal stromal cancer	20470368	CNVD
Adenoid cystic carcinoma	17372589	CNVD
Myelofibrosis	22110671	CNVD
Breast cancer	17603634	CNVD
Cancer	21183584	CNVD
Hirschsprung''s Disease	21712996	CNVD
Lissencephaly	21572526	CNVD
Lung cancer	18438408	CNVD
Acute myeloid leukemia	21251322	CNVD
small cell lung cancer	20016488	CNVD
Autism	20858243	CNVD
Malignant peripheral nerve sheath tumor	18522746	CNVD
Adenoid cystic carcinoma	18698036	CNVD
Breast cancer	19602461	CNVD
Breast cancer	17899364	CNVD
Cancer	20164920	CNVD
Colorectal cancer	16272173	CNVD
Breast cancer	21364760	CNVD

Chromatin state (count:443 , 50 per page) page: 1 2 3 4 5 6 7 ... 9

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr12:40466400-40498200	Weak transcription	Breast variant Human Mammary Epithelial Cells (vHMEC)	Breast
2	chr12:40471400-40496800	Weak transcription	Stomach Smooth Muscle	stomach
3	chr12:40474400-40497000	Weak transcription	Ovary	ovary
4	chr12:40475400-40497200	Weak transcription	HUES48 Cell Line	embryonic stem cell
5	chr12:40476400-40497400	Weak transcription	H9 Derived Neuronal Progenitor Cultured Cells	ES cell derived
6	chr12:40476600-40498400	Weak transcription	Fetal Stomach	stomach
7	chr12:40476800-40497800	Weak transcription	ES-UCSF4 Cell Line	embryonic stem cell
8	chr12:40477000-40497000	Weak transcription	iPS-15b Cell Line	embryonic stem cell
9	chr12:40477400-40496800	Weak transcription	HUES64 Cell Line	embryonic stem cell
10	chr12:40480600-40496800	Weak transcription	Brain Dorsolateral Prefrontal Cortex	brain
11	chr12:40482000-40497800	Weak transcription	ES-WA7 Cell Line	embryonic stem cell
12	chr12:40485600-40496800	Weak transcription	Primary hematopoietic stem cells short term culture	blood
13	chr12:40487000-40497400	Weak transcription	Monocytes-CD14+_RO01746	blood
14	chr12:40488200-40498600	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell
15	chr12:40491000-40497000	Weak transcription	H9 Derived Neuron Cultured Cells	ES cell derived
16	chr12:40492400-40498600	Weak transcription	iPS DF 6.9 Cell Line	embryonic stem cell
17	chr12:40492800-40496800	Weak transcription	Pancreas	Pancrea
18	chr12:40492800-40497600	Weak transcription	Left Ventricle	heart
19	chr12:40492800-40498000	Weak transcription	Gastric	stomach
20	chr12:40492800-40498600	Weak transcription	H1 BMP4 Derived Trophoblast Cultured Cells	ES cell derived
21	chr12:40492800-40498600	Weak transcription	H1 Derived Mesenchymal Stem Cells	ES cell derived
22	chr12:40492800-40498600	Weak transcription	Lung	lung
23	chr12:40493600-40496800	Weak transcription	H1 BMP4 Derived Mesendoderm Cultured Cells	ES cell derived
24	chr12:40493600-40497000	Weak transcription	Brain Anterior Caudate	brain
25	chr12:40493600-40497000	Weak transcription	Fetal Kidney	kidney
26	chr12:40493800-40497400	Weak transcription	Primary hematopoietic stem cells G-CSF-mobilized Female	--
27	chr12:40493800-40497400	Weak transcription	Fetal Heart	heart
28	chr12:40494000-40496800	Weak transcription	Duodenum Mucosa	Duodenum
29	chr12:40494000-40496800	Weak transcription	HepG2	liver
30	chr12:40494000-40497000	Weak transcription	Liver	Liver
31	chr12:40494000-40497000	Weak transcription	Duodenum Smooth Muscle	Duodenum
32	chr12:40494200-40496800	Weak transcription	Brain Cingulate Gyrus	brain
33	chr12:40494200-40496800	Weak transcription	Fetal Intestine Small	intestine
34	chr12:40494200-40496800	Enhancers	K562	blood
35	chr12:40494200-40498000	Weak transcription	Fetal Lung	lung
36	chr12:40494200-40498200	Weak transcription	A549	lung
37	chr12:40494400-40496800	Weak transcription	Ganglion Eminence derived primary cultured neurospheres	brain
38	chr12:40494400-40497000	Weak transcription	Mesenchymal Stem Cell Derived Chondrocyte Cultured Cells	embryonic stem cell
39	chr12:40494600-40496800	Weak transcription	Rectal Mucosa Donor 31	rectum
40	chr12:40494600-40497000	Weak transcription	Stomach Mucosa	stomach
41	chr12:40494600-40498000	Weak transcription	NHLF	lung
42	chr12:40495200-40497400	Enhancers	Fetal Adrenal Gland	Adrenal Gland
43	chr12:40495400-40497000	Enhancers	HUES6 Cell Line	embryonic stem cell
44	chr12:40495400-40498000	Enhancers	Small Intestine	intestine
45	chr12:40495800-40496800	Weak transcription	Pancreatic Islets	Pancreatic Islet
46	chr12:40495800-40497000	Weak transcription	Foreskin Melanocyte Primary Cells skin01	Skin
47	chr12:40495800-40497000	Weak transcription	Hela-S3	cervix
48	chr12:40495800-40497600	Weak transcription	iPS-18 Cell Line	embryonic stem cell
49	chr12:40495800-40497600	Enhancers	Colon Smooth Muscle	Colon
50	chr12:40496000-40496800	Enhancers	Cortex derived primary cultured neurospheres	brain

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